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Volumn 59, Issue 45, 2003, Pages 8855-8858

Application of phenolic oxidation chemistry in synthesis: Preparation of the BCE ring system of ryanodine

Author keywords

Phenolic oxidation; Ryanodine

Indexed keywords

BICYCLO COMPOUND; NATURAL PRODUCT; PHENOL; RYANODINE; SINGLET OXYGEN;

EID: 0142248468     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2003.05.001     Document Type: Article
Times cited : (30)

References (16)
  • 13
    • 85030968708 scopus 로고    scopus 로고
    • 7 to chromatographic purification
    • The low isolated yield is due to instability of 7 to chromatographic purification.
  • 14
    • 0034597522 scopus 로고    scopus 로고
    • The only comparable reaction sequence that we are aware of occurs in Danishefsky's elegant work towards the total synthesis of lactonamycin, see:
    • The only comparable reaction sequence that we are aware of occurs in Danishefsky's elegant work towards the total synthesis of lactonamycin, see: Cox C., Danishefsky S. J. Org. Lett. 2:2000;3493.
    • (2000) J. Org. Lett. , vol.2 , pp. 3493
    • Cox, C.1    Danishefsky, S.2
  • 15
    • 85030957375 scopus 로고    scopus 로고
    • Although the structure of this product has yet to be fully delineated, spectroscopic evidence is consistent with ii , a product derived from acetonitrile adduct i
    • Although the structure of this product has yet to be fully delineated, spectroscopic evidence is consistent with ii , a product derived from acetonitrile adduct i.
  • 16
    • 85030961966 scopus 로고    scopus 로고
    • 1H NMR analysis
    • 1H NMR analysis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.